돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 41302생성일: 2026년 10월 24일

4-Chlorobenzenesulfonyl chloride → (3R)-1-[(4-chlorophenyl)sulfonyl]-3-methylpiperazine

https://huagongshe.com/ko/reaction/41302

반응식

참여 물질

역할이름HCID투입량
반응물4-Chlorobenzenesulfonyl chlorideHCID 7398—
반응물TriethylamineHCID 8471—
반응물tert-Butyl (2R)-2-methylpiperazine-1-carboxylateHCID 10262201—
용매DichloromethaneHCID 6344—
생성물(3R)-1-[(4-chlorophenyl)sulfonyl]-3-methylpiperazineHCID 1163046578.7%

반응 단계

To a solution of 1,1-dimethylethyl (2R)-2-methyl-1-piperazinecarboxylate (1.5 g, 07.5 mmol) in dry DCM (40 mL) was added triethylamine (2.59 mL, 18.8 mmol) and 4-chlorobenzenesulfonyl chloride (3.15 g, 10.5 mmol) and the reaction stirred at room temperature for 48 h. To the reaction was added resin supported-triamine (5 g) and the mixture stirred for 4 h. The reaction mixture was filtered and the filtrate washed with 0.5 M HCl (aq., 100 mL) followed by water (100 mL) before it was dried (MgSO4), filtered and the solvent removed in vacuo. The crude product was dissolved in DCM (40 mL) and TFA (10 mL) was added. The solution was stirred for 20 min. The solvent was evaporated and the residue tajen up in DCM (40 mL) and washed with 50% aqueous sodium bicarbonate (100 mL) followed by water (100 mL). The organic phase was dried (MgSO4), filtered and the solvent removed in vacuo to give the title compound (1.62 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08530478B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-d72421402bcd411a95caa05e81703400
출처 메모uspto-grants-2013_09